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超声分子成像:迈向临床转化。

Ultrasound molecular imaging: Moving toward clinical translation.

作者信息

Abou-Elkacem Lotfi, Bachawal Sunitha V, Willmann Jürgen K

机构信息

Department of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine, Stanford, CA, USA.

Department of Radiology, Molecular Imaging Program at Stanford, Stanford University, School of Medicine, Stanford, CA, USA.

出版信息

Eur J Radiol. 2015 Sep;84(9):1685-93. doi: 10.1016/j.ejrad.2015.03.016. Epub 2015 Mar 21.

Abstract

Ultrasound is a widely available, cost-effective, real-time, non-invasive and safe imaging modality widely used in the clinic for anatomical and functional imaging. With the introduction of novel molecularly-targeted ultrasound contrast agents, another dimension of ultrasound has become a reality: diagnosing and monitoring pathological processes at the molecular level. Most commonly used ultrasound molecular imaging contrast agents are micron sized, gas-containing microbubbles functionalized to recognize and attach to molecules expressed on inflamed or angiogenic vascular endothelial cells. There are several potential clinical applications currently being explored including earlier detection, molecular profiling, and monitoring of cancer, as well as visualization of ischemic memory in transient myocardial ischemia, monitoring of disease activity in inflammatory bowel disease, and assessment of arteriosclerosis. Recently, a first clinical grade ultrasound contrast agent (BR55), targeted at a molecule expressed in neoangiogenesis (vascular endothelial growth factor receptor type 2; VEGFR2) has been introduced and safety and feasibility of VEGFR2-targeted ultrasound imaging is being explored in first inhuman clinical trials in various cancer types. This review describes the design of ultrasound molecular imaging contrast agents, imaging techniques, and potential future clinical applications of ultrasound molecular imaging.

摘要

超声是一种广泛应用、经济高效、实时、无创且安全的成像方式,在临床上广泛用于解剖和功能成像。随着新型分子靶向超声造影剂的引入,超声的另一个维度成为现实:在分子水平上诊断和监测病理过程。最常用的超声分子成像造影剂是微米级含气微泡,其功能化后可识别并附着于炎症或血管生成性血管内皮细胞上表达的分子。目前正在探索几种潜在的临床应用,包括癌症的早期检测、分子剖析和监测,以及短暂性心肌缺血中缺血记忆的可视化、炎症性肠病中疾病活动的监测和动脉硬化的评估。最近,一种针对新生血管生成中表达的分子(血管内皮生长因子受体2型;VEGFR2)的首个临床级超声造影剂(BR55)已被引入,并且正在各种癌症类型的首次人体临床试验中探索VEGFR2靶向超声成像的安全性和可行性。本综述描述了超声分子成像造影剂的设计、成像技术以及超声分子成像潜在的未来临床应用。

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